A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972575



Internal ID22747510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123881229..123881229hg38UCSC Ensembl
chr10:125640745..125640745hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368530
Samples
Known GenesCPXM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972575
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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